Trimethyl 2-bromobenzene-1,3,5-tricarboxylate CAS 43141-00-0

Purity 97%+In StockPharmaceutical Standards
CAS No.43141-00-0
Molecular FormulaC12H11BrO6
Molecular Weight331.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Trimethyl 2-bromobenzene-1,3,5-tricarboxylate CAS 43141-00-0 chemical structure

Description

CATO manufactures Trimethyl 2-bromobenzene-1,3,5-tricarboxylate under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

CATO supplies Trimethyl 2-bromobenzene-1,3,5-tricarboxylate (CAS 43141-00-0), a certified reference material (molecular formula C12H11BrO6, MW 331.12 g/mol) for analytical method development and quality control.

The molecular framework of Trimethyl 2-bromobenzene-1,3,5-tricarboxylate (C12H11BrO6) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC12H11BrO6
Molecular Weight331.12 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1969
Halogen ContentBr-containing

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